{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["3(6)"],"submitter":["Rohli KE"],"pubmed_abstract":["Defects in the pancreatic β-cell's secretion system are well-described in type 2 diabetes (T2D) and include impaired proinsulin processing and a deficit in mature insulin-containing secretory granules; however, the cellular mechanisms underlying these defects remain poorly understood. To address this, we used an in situ fluorescent pulse-chase strategy to study proinsulin trafficking. We show that insulin granule formation and the appearance of nascent granules at the plasma membrane are decreased in rodent and cell culture models of prediabetes and hyperglycemia. Moreover, we link the defect in insulin granule formation to an early trafficking delay in endoplasmic reticulum (ER) export of proinsulin, which is independent of overt ER stress. Using a ratiometric redox sensor, we show that t"],"journal":["Function (Oxford, England)"],"pagination":["zqac051"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9614934"],"repository":["biostudies-literature"],"pubmed_title":["ER Redox Homeostasis Regulates Proinsulin Trafficking and Insulin Granule Formation in the Pancreatic Islet β-Cell."],"pmcid":["PMC9614934"],"pubmed_authors":["Boyer CK","Bauchle CJ","Stephens SB","Zhang J","Bearrows SC","Elison WS","Rohli KE","Wang Y","Moyer MR","Blom SE"],"additional_accession":[]},"is_claimable":false,"name":"ER Redox Homeostasis Regulates Proinsulin Trafficking and Insulin Granule Formation in the Pancreatic Islet β-Cell.","description":"Defects in the pancreatic β-cell's secretion system are well-described in type 2 diabetes (T2D) and include impaired proinsulin processing and a deficit in mature insulin-containing secretory granules; however, the cellular mechanisms underlying these defects remain poorly understood. To address this, we used an in situ fluorescent pulse-chase strategy to study proinsulin trafficking. We show that insulin granule formation and the appearance of nascent granules at the plasma membrane are decreased in rodent and cell culture models of prediabetes and hyperglycemia. Moreover, we link the defect in insulin granule formation to an early trafficking delay in endoplasmic reticulum (ER) export of proinsulin, which is independent of overt ER stress. Using a ratiometric redox sensor, we show that t","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2025-04-18T20:40:01.421Z","creation":"2025-04-07T08:44:20.453Z"},"accession":"S-EPMC9614934","cross_references":{"pubmed":["36325514"],"doi":["10.1093/function/zqac051"]}}